Biomol Ther.  2015 May;23(3):225-232. 10.4062/biomolther.2014.136.

Antitumor Effects of Fucoidan on Human Colon Cancer Cells via Activation of Akt Signaling

• Han YS
• Lee JH
• Lee SH

• KMID: 2380331
• DOI: http://doi.org/10.4062/biomolther.2014.136

Abstract

We identified a novel Akt signaling mechanism that mediates fucoidan-induced suppression of human colon cancer cell (HT29) proliferation and anticancer effects. Fucoidan treatment significantly inhibited growth, induced G1-phase-associated upregulation of p21WAF1 expression, and suppressed cyclin and cyclin-dependent kinase expression in HT29 colon cancer cells. Additionally, fucoidan treatment activated the Akt signaling pathway, which was inhibited by treatment with an Akt inhibitor. The inhibition of Akt activation reversed the fucoidan-induced decrease in cell proliferation, the induction of G1-phase-associated p21WAF1 expression, and the reduction in cell cycle regulatory protein expression. Intraperitoneal injection of fucoidan reduced tumor volume; this enhanced antitumor efficacy was associated with induction of apoptosis and decreased angiogenesis. These data suggest that the activation of Akt signaling is involved in the growth inhibition of colon cancer cells treated with fucoidan. Thus, fucoidan may serve as a potential therapeutic agent for colon cancer.

Keyword

Anticancer effect; Cell cycle arrest; Fucoidan; Human colorectal cancer cells

MeSH Terms

Apoptosis
Cell Cycle
Cell Cycle Checkpoints
Cell Proliferation
Colonic Neoplasms*
Cyclins
Humans
Injections, Intraperitoneal
Phosphotransferases
Tumor Burden
Up-Regulation
Cyclins
Phosphotransferases